FDA Inspection 897363 — Augusta Medical Systems, LLC

Augusta Medical Systems, LLC — FEI 3003038113

The FDA completed an inspection of Augusta Medical Systems, LLC on July 22, 2014 in Augusta, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 22, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Augusta, GA (United States)

Citations

IDCFRDescription
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
312721 CFR 820.80(e)Documentation